Ret Bladder Liquid
NDC Package 63083-7006-1
Package Information
Ret Bladder liquids is temporarily relieves passiveness or being weak-willed, lacking confidence or trust in ones self, mental weariness, staleness in life, self-pity, bitterness, grief, despair, or sadness.*. This formulation utilizes a liquid delivery system. Marketed by Professional Complementary Health Formulas, this product is identified by NDC 63083-7006.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 30 [hp_X]/29.5mL
- APIS MELLIFERA 30 [hp_X]/29.5mL
- ARTEMISIA CINA PRE-FLOWERING TOP 30 [hp_X]/29.5mL
- CARPINUS BETULUS FLOWER 3 [hp_X]/29.5mL
- CENTAURIUM ERYTHRAEA FLOWERING TOP 3 [hp_X]/29.5mL
- CERATOSTIGMA WILLMOTTIANUM FLOWERING TOP 3 [hp_X]/29.5mL
- DELPHINIUM STAPHISAGRIA SEED 30 [hp_X]/29.5mL
- POTASSIUM ALUM 30 [hp_X]/29.5mL
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM 3 [hp_X]/29.5mL
- PULSATILLA MONTANA WHOLE 30 [hp_X]/29.5mL
- SALIX ALBA FLOWERING TOP 3 [hp_X]/29.5mL
- SEPIA OFFICINALIS JUICE 30 [hp_X]/29.5mL
- SODIUM CHLORIDE 3 [hp_X]/29.5mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 30 [hp_X]/29.5mL
- VERATRUM ALBUM ROOT 30 [hp_X]/29.5mL
Regulatory & Marketing
Hierarchy Structure
- 63083 - Professional Complementary Health Formulas
- 63083-7006 - Ret Bladder
- 63083-7006-1 - 29.5 mL in 1 BOTTLE, DROPPER
- 63083-7006 - Ret Bladder
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 63083-7006-1 identifies a specific commercial package of 29.5 ml in 1 bottle, dropper of Ret Bladder 7006, a human over the counter drug labeled by Professional Complementary Health Formulas. This liquid is formulated for oral use and contains activated charcoal; apis mellifera; artemisia cina pre-flowering top; carpinus betulus flower; centaurium erythraea flowering top; ceratostigma willmottianum flowering top; delphinium staphisagria seed; potassium alum; potassium phosphate, unspecified form; pulsatilla montana whole; salix alba flowering top; sepia officinalis juice; sodium chloride; spongia officinalis skeleton, roasted; veratrum album root as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Professional Complementary Health Formulas on August 15, 1984. The current certification is valid through December 31, 2027.
How is this Professional Complementary Health Formulas product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 63083700601. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.